Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/53992
Title: Mephedrone pharmacokinetics after intravenous and oral administration in rats: relation to pharmacodynamics
Author: Martínez-Clemente, José
López-Arnau, Raúl
Carbó Banús, Marcel·lí
Pubill Sánchez, David
Camarasa García, Jordi
Escubedo Rafa, Elena
Keywords: Amfetamines
Sistema nerviós central
Cervell
Farmacocinètica
Efectes fisiològics
Drogues de disseny
Amphetamines
Central nervous system
Brain
Pharmacokinetics
Physiological effect
Designer drugs
Issue Date: 7-May-2013
Publisher: Springer Verlag
Abstract: Rationale Mephedrone (4-methylmethcathinone) is a still poorly known drug of abuse, alternative to ecstasy or cocaine. Objective The major aims were to investigate the pharmacokineticsa and locomotor activity of mephedrone in rats and provide a pharmacokinetic/pharmacodynamic model. Methods Mephedrone was administered to male Sprague-Dawley rats intravenously (10 mg/kg) and orally (30 and 60 mg/kg). Plasma concentrations and metabolites were characterized using LC/MS and LC-MS/MS fragmentation patterns. Locomotor activity was monitored for 180-240 min. Results Mephedrone plasma concentrations after i.v. administration fit a two-compartment model (α=10.23 h−1, β=1.86 h−1). After oral administration, peak mephedrone concentrations were achieved between 0.5 and 1 h and declined to undetectable levels at 9 h. The absolute bioavailability of mephedrone was about 10 % and the percentage of mephedrone protein binding was 21.59±3.67%. We have identified five phase I metabolites in rat blood after oral administration. The relationship between brain levels and free plasma concentration was 1.85±0.08. Mephedrone induced a dose-dependent increase in locomotor activity, which lasted up to 2 h. The pharmacokinetic-pharmacodynamic model successfully describes the relationship between mephedrone plasma concentrations and its psychostimulant effect. Conclusions We suggest a very important first-pass effect for mephedrone after oral administration and an easy access to the central nervous system. The model described might be useful in the estimation and prediction of the onset, magnitude,and time course of mephedrone pharmacodynamics as well as to design new animal models of mephedrone addiction and toxicity.
Note: Fe d'errates disponible a: http://​dx.​doi.​org/​10.​1007/​s00213-013-3283-6
Note: Versió postprint del document publicat a: http://dx.doi.org/10.1007/s00213-013-3108-7
It is part of: Psychopharmacology, 2013, vol. 229, num. 2, p. 295-306
Related resource: http://dx.doi.org/10.1007/s00213-013-3108-7
http://​dx.​doi.​org/​10.​1007/​s00213-013-3283-6
URI: http://hdl.handle.net/2445/53992
ISSN: 0033-3158
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

Files in This Item:
File Description SizeFormat 
622132.pdf303.84 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.